Weekly reads: MYC phosphorylation, reverse protein aging, mitochondria don’t like space, that peptide committee

Why am I interested in MYC phosphorylation? What is MYC?

Long-time readers of The Niche probably remember that  the MYC family is one of my primary interests. These proteins are essential for normal development (and stem cell function) as well as contributing to the formation of many tumors when overexpressed or mutated. MYC was also one of the original four Yamanaka factors for reprogramming.

Rosalie Sears, MYC phosphorylation
Rosalie Sears’ lab has an interesting new paper on MYC phosphorylation. Photo (OHSU/Christine Torres Hicks).

MYC’s behavior as a protein is in part controlled by its phosphorylation, which in part works to regulate the levels of MYC family proiteins. A new paper describes an interesting function of one particular kind of MYC phosphorylation at S62. A common mutation in cancer, MYC T58A, prevents normal phosphorylation at that site, locking MYC in a stable, highly active state with persistent serine 62 phosphorylation. The new paper from Rosalie Sears provides new insights into the functions of that S62 phosphorylation. We’ll start there.

Recommended reads

Aging research

PCAC, BPC-157
PCAC BPC-157 vote. Screenshot from FDA meeting.

Conflicted PCAC recommends most of the peptides that RFK Jr. wants “freed”

Watching this meeting was both interesting and kind of painful because most of the time most of the PCAC members ignored what the FDA experts had to say about these unproven peptide drugs.

Also, as I wrote before, this PCAC has many members who stand to gain from their own votes on peptides. How is that OK? It’s not, but at this HHS, COIs don’t matter.

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